CR20210098A - COMPUESTOS DE PIRAZOLO[3,4-b]PIRIDINA COMO INHIBIDORES DE CINASAS TAM Y MET - Google Patents

COMPUESTOS DE PIRAZOLO[3,4-b]PIRIDINA COMO INHIBIDORES DE CINASAS TAM Y MET

Info

Publication number
CR20210098A
CR20210098A CR20210098A CR20210098A CR20210098A CR 20210098 A CR20210098 A CR 20210098A CR 20210098 A CR20210098 A CR 20210098A CR 20210098 A CR20210098 A CR 20210098A CR 20210098 A CR20210098 A CR 20210098A
Authority
CR
Costa Rica
Prior art keywords
sup
tam
inhibitors
pyrazolo
pyridine compounds
Prior art date
Application number
CR20210098A
Other languages
English (en)
Inventor
Shelley Allen
Ellen Laird
Adam Cook
Qian Zhao
Ronald Jay Hinklin
Joshua Dahlke
John Gaudino
Oren T Mcnulty
Patrick Barbour
Original Assignee
Array Biopharma Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Array Biopharma Inc filed Critical Array Biopharma Inc
Publication of CR20210098A publication Critical patent/CR20210098A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

La presente invención se refiere a compuestos de la Fórmula <strong>I</strong>: y estereoisómeros, tautómeros y sales de los mismos farmacéuticamente aceptables, en donde R<sup>1</sup>, R<sup>2</sup>, R<sup>9</sup>, X<sup>1</sup> y G son como se definen en la presente, los cuales son inhibidores de una o más cinasas TAM y/o cinasa c-Met, y son útiles en el tratamiento y prevención de enfermedades las cuales pueden ser tratadas con un inhibidor de cinasa TAM y/o un inhibidor de cinasa c-Met.
CR20210098A 2018-08-30 2019-08-29 COMPUESTOS DE PIRAZOLO[3,4-b]PIRIDINA COMO INHIBIDORES DE CINASAS TAM Y MET CR20210098A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862724829P 2018-08-30 2018-08-30
US201962858686P 2019-06-07 2019-06-07
PCT/US2019/048701 WO2020047184A1 (en) 2018-08-30 2019-08-29 PYRAZOLO[3,4-b]PYRIDINE COMPOUNDS AS INHIBITORS OF TAM AND MET KINASES

Publications (1)

Publication Number Publication Date
CR20210098A true CR20210098A (es) 2021-07-01

Family

ID=67928919

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20210098A CR20210098A (es) 2018-08-30 2019-08-29 COMPUESTOS DE PIRAZOLO[3,4-b]PIRIDINA COMO INHIBIDORES DE CINASAS TAM Y MET

Country Status (24)

Country Link
US (3) US11104676B2 (es)
EP (1) EP3843850B1 (es)
JP (2) JP6970859B2 (es)
KR (1) KR20210049898A (es)
CN (1) CN112930215A (es)
AU (3) AU2019330017B2 (es)
BR (1) BR112021002722A2 (es)
CA (1) CA3110502C (es)
CL (1) CL2021000467A1 (es)
CO (1) CO2021002651A2 (es)
CR (1) CR20210098A (es)
CU (1) CU20210015A7 (es)
DO (1) DOP2021000038A (es)
EC (1) ECSP21012498A (es)
IL (1) IL281127B2 (es)
MA (1) MA53487A (es)
MX (1) MX2021001952A (es)
NI (1) NI202100007A (es)
PE (1) PE20211779A1 (es)
PH (1) PH12021500017A1 (es)
SG (1) SG11202101148UA (es)
TW (1) TW202024071A (es)
UY (1) UY38349A (es)
WO (1) WO2020047184A1 (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2019323455A1 (en) * 2018-08-24 2021-04-01 Transthera Sciences (Nanjing), Inc. Novel quinoline derivative inhibitor
TWI817018B (zh) 2019-06-28 2023-10-01 美商艾瑞生藥股份有限公司 用於治療braf相關的疾病和失調症之化合物
AU2020342108B2 (en) * 2019-09-06 2024-03-07 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Compound having Axl and c-Met kinase inhibitory activity, preparation thereof and application thereof
TW202115028A (zh) * 2019-09-24 2021-04-16 大陸商南京藥捷安康生物科技有限公司 雜環衍生物及其用途
AU2021231435A1 (en) * 2020-03-03 2022-09-22 Array Biopharma Inc. Methods to treat cancer using (R)-N-(3-fluoro-4-((3-((1-hydroxypropan-2-yl)amino)-1H-pyrazolo(3,4-b)pyridin-4-yl)oxy)phenyl)-3-(4-fluorophenyl)-1-isopropyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxamide
CA3214399A1 (en) * 2021-04-09 2022-10-13 Frank Perabo Treatment of cancer with kdm4 inhibitors
WO2023002360A1 (en) 2021-07-22 2023-01-26 Pfizer Inc. Solid forms and formulations of an inhibitor of tam and c-met kinases
IT202100022682A1 (it) * 2021-09-01 2023-03-01 Luigi Frati Derivati pirimidinici e loro uso nel trattamento di tumori
CN115850301A (zh) * 2021-09-24 2023-03-28 中山医诺维申新药研发有限公司 吡唑酮类化合物及其组合物和用途
WO2023078408A1 (zh) * 2021-11-05 2023-05-11 上海海和药物研究开发股份有限公司 含met受体酪氨酸激酶抑制剂的药物组合及应用
CA3236956A1 (en) * 2021-11-05 2023-05-11 Haihe Biopharma Co., Ltd. Solid dispersion, preparation method therefor, and solid formulation comprising same
US11753395B2 (en) 2021-12-16 2023-09-12 Kinnate Biopharma Inc. Inhibitors of MET kinase
CN116003406B (zh) * 2021-12-29 2024-01-23 北京鞍石生物科技有限责任公司 杂芳环氮氧化合物及其制备方法和应用
TW202340177A (zh) 2021-12-30 2023-10-16 美商拜歐米富士恩股份有限公司 作為 flt3抑制劑之吡嗪化合物
CN116768868B (zh) * 2023-08-15 2023-12-08 云南省药物研究所 一种哒嗪酮硫代衍生物及其制备方法和应用

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773919A (en) 1969-10-23 1973-11-20 Du Pont Polylactide-drug mixtures
US7173031B2 (en) 2004-06-28 2007-02-06 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
CA2572331A1 (en) 2004-07-02 2006-02-09 Exelixis, Inc. C-met modulators and method of use
PE20061119A1 (es) 2005-01-19 2006-11-27 Aventis Pharma Sa PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie
US7723330B2 (en) 2006-03-07 2010-05-25 Array Biopharma Inc. Heterobicyclic pyrazole compounds and methods of use
CN102816175B (zh) 2011-06-09 2015-12-16 上海汇伦生命科技有限公司 一种杂环并吡啶酮类化合物,其中间体、制备方法和用途
WO2013032797A2 (en) * 2011-08-26 2013-03-07 New Hope R & D Bioscience, Inc. Oxetane 3,3-dicarboxamide compounds and methods of making and using same
BR112014006419A2 (pt) * 2011-09-19 2018-08-07 Genentech Inc métodos para tratar um paciente com câncer, kit e artigo
AU2012339640B2 (en) 2011-11-14 2017-01-05 Ignyta, Inc. Uracil derivatives as AXL and c-MET kinase inhibitors
TW201536291A (zh) 2013-08-02 2015-10-01 Cephalon Inc 單獨使用AXL/cMET抑制劑或與其它藥劑組合使用以治療多種癌症之方法
CA2934667A1 (en) * 2013-12-26 2015-07-02 Ignyta, Inc. Pyrazolo[1,5-a]pyridine derivatives and methods of their use
WO2016004305A2 (en) 2014-07-02 2016-01-07 Pharmacyclics Llc Inhibitors of bruton's tyrosine kinase
WO2016016822A1 (en) 2014-07-31 2016-02-04 Novartis Ag Combination therapy
GB201509338D0 (en) 2015-05-29 2015-07-15 Bergenbio As Combination therapy
KR101829998B1 (ko) 2015-11-04 2018-02-19 롬엔드하스전자재료코리아유한회사 착색 감광성 수지 조성물 및 이를 이용한 차광성 스페이서
SI3436461T1 (sl) * 2016-03-28 2024-03-29 Incyte Corporation Pirolotriazinske spojine kot tam-inhibitorji
EP3490676A1 (en) 2016-07-29 2019-06-05 Eli Lilly and Company Combination therapy with merestinib and anti-pd-l1 or anti-pd-1 inhibitors for use in the treatment of cancer
CN109689056A (zh) 2016-08-01 2019-04-26 亚尼塔公司 用于治疗癌症的组合
WO2018039275A1 (en) 2016-08-24 2018-03-01 Ignyta, Inc. Combinations for the treatment of cancer
EP3541384A1 (en) 2016-11-16 2019-09-25 Eli Lilly and Company Treatment of cancer with exon 14 skipping mutation(s) or exon 14 skipping phenotype
CN108250200A (zh) 2016-12-28 2018-07-06 中国科学院上海药物研究所 一种具有Axl抑制活性的化合物及其制备和应用
JOP20180040A1 (ar) 2017-04-20 2019-01-30 Gilead Sciences Inc مثبطات pd-1/pd-l1
EP3719012B1 (en) 2017-11-24 2024-03-06 Medshine Discovery Inc. N-[4-[(2-amino-4-pyridinyl)oxy]-3-fluorophenyl]-3-(4-fluorophenyl)-1,2,3,4-tetrahydro-2,4-dioxo-5-pyrimidinecarboxamide derivatives as c-met/axl inhibitors for the treatment of tumors
US11247990B1 (en) 2017-12-07 2022-02-15 Array Biopharma Inc Bicyclic fused pyridine compounds as inhibitors of TAM kinases

Also Published As

Publication number Publication date
AU2022202946B2 (en) 2023-08-03
AU2022221514B2 (en) 2023-11-02
IL281127B1 (en) 2023-12-01
AU2019330017B2 (en) 2022-05-26
PE20211779A1 (es) 2021-09-08
JP6970859B2 (ja) 2021-11-24
US20230011441A1 (en) 2023-01-12
JP2021527114A (ja) 2021-10-11
TW202024071A (zh) 2020-07-01
MA53487A (fr) 2021-12-08
CA3110502C (en) 2023-10-03
EP3843850A1 (en) 2021-07-07
IL281127B2 (en) 2024-04-01
NI202100007A (es) 2021-06-22
UY38349A (es) 2020-03-31
CN112930215A (zh) 2021-06-08
ECSP21012498A (es) 2021-03-31
IL281127A (en) 2021-04-29
DOP2021000038A (es) 2021-04-15
SG11202101148UA (en) 2021-04-29
US11104676B2 (en) 2021-08-31
EP3843850B1 (en) 2023-11-15
CO2021002651A2 (es) 2021-03-08
US11780835B2 (en) 2023-10-10
CA3110502A1 (en) 2020-03-05
US20240174666A1 (en) 2024-05-30
JP7337133B2 (ja) 2023-09-01
AU2022202946A1 (en) 2022-05-26
CL2021000467A1 (es) 2021-10-22
BR112021002722A2 (pt) 2021-08-10
US20200079770A1 (en) 2020-03-12
KR20210049898A (ko) 2021-05-06
MX2021001952A (es) 2021-04-19
JP2022009720A (ja) 2022-01-14
CU20210015A7 (es) 2021-10-12
AU2019330017A1 (en) 2021-03-04
WO2020047184A1 (en) 2020-03-05
PH12021500017A1 (en) 2021-09-13
AU2022221514A1 (en) 2022-09-22

Similar Documents

Publication Publication Date Title
MX2021001952A (es) Compuestos de pirazolo[3,4-b]piridina como inhibidores de cinasas tam y met.
TN2019000110A1 (en) Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
TN2019000107A1 (en) Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
PH12018500121A1 (en) Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
NZ744349A (en) Pyrazolo[1,5-a]pyrazin-4-yl derivatives as jak-inhibitors
JOP20210301A1 (ar) بيرولات ثلاثية الحلقة مكثفة كمُعدِّلات مضاد تريبسين ألفا-1
MX2009006756A (es) Derivados de 1-amino-metil-l-fenil-ciclohexano como inhibidores de dpp-iv.
EA201691428A1 (ru) Бициклические гетероциклические производные в качестве ингибиторов irak4
MX2017013797A (es) Inhibidor de janus quinasa.
UA106054C2 (uk) ЗАМІЩЕНІ ПІРАЗОЛО[1,5-a]ПІРИМІДИНОВІ СПОЛУКИ ЯК ІНГІБІТОРИ TРK-КІНАЗИ
WO2014106800A3 (en) Substituted 2-amino pyrimidine derivatives as kinase inhibitors
MX2017009600A (es) Derivados de 2-fenil-3h-imidazo[4,5-b]piridina utiles como inhibidores de actividad de receptor huerfano similar a tirosina cinasa (ror1) de tirosina cinasa de mamifero.
CR20210364A (es) Compuestos de quinolina como inhibidores de quinasas tam y met
MX2015012896A (es) Inhibidores de pirrolo [2,3-b] piridina cdk9 cinasa.
MX2021006011A (es) Un inhibidor de la quinasa aurora a para su uso en el tratamiento del neuroblastoma.
EA202190393A1 (ru) СОЕДИНЕНИЯ ПИРАЗОЛО[3,4-b]ПИРИДИНА В КАЧЕСТВЕ ИНГИБИТОРОВ TAM- И Met-КИНАЗ
MY156466A (en) Aminothiazoles and their uses
EA201990939A1 (ru) ЗАМЕЩЕННЫЕ ПИРАЗОЛО[1,5-a]ПИРИДИНОВЫЕ СОЕДИНЕНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ RET КИНАЗЫ
EA201990940A1 (ru) ЗАМЕЩЕННЫЕ ПИРАЗОЛО[1,5-a]ПИРИДИНОВЫЕ СОЕДИНЕНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ RET КИНАЗЫ
MX2020008273A (es) Inhibidores de la cinasa del complejo de activacion transcripcional notch (&#34;nack&#34;) y metodos para el uso de los mismos.
UA100999C2 (ru) Аминотиазолы и их применение